Canonical Allele Identifier: CA410739645

Gene: SCARF2

Linked Data

• gnomAD v4: 22-20425908-C-A
• MyVariant Identifiers: chr22:g.20780195C>A (hg19) ; chr22:g.20425908C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425908C>A , CM000684.2:g.20425908C>A	GRCh38
NC_000022.10:g.20780195C>A , CM000684.1:g.20780195C>A	GRCh37
NC_000022.9:g.19110195C>A	NCBI36
NG_031868.2:g.16952G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2068G>T MANE Select	ENSP00000477564.2:p.Ala690Ser
ENST00000615031.4:c.2083G>T	ENSP00000479389.1:p.Ala695Ser
ENST00000622235.4:c.2068G>T	ENSP00000477564.1:p.Ala690Ser
ENST00000623402.1:c.2083G>T	ENSP00000485276.1:p.Ala695Ser
NM_153334.6:c.2083G>T	NP_699165.3:p.Ala695Ser
NM_182895.4:c.2068G>T	NP_878315.2:p.Ala690Ser
NM_153334.7:c.2083G>T	NP_699165.3:p.Ala695Ser
NM_182895.5:c.2068G>T MANE Select	NP_878315.2:p.Ala690Ser